THERAPEUTIC STIMULATOR 2100 (TS-2100)

THERAPEUTIC STIMULATOR 2100 (TS-2100) is an FDA 510(k)-cleared medical device (K914904) manufactured by Myo/Kinetic Systems, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 27, 1992. Regulation: 8.